Generic Structures of Cytotoxic Liprotides: Nano‐Sized Complexes with Oleic Acid Cores and Shells of Disordered Proteins

The cytotoxic complex formed between α‐lactalbumin and oleic acid (OA) has inspired many studies on protein–fatty acid complexes, but structural insight remains sparse. After having used small‐angle X‐ray scattering (SAXS) to obtain structural information, we present a new, generic structural model of cytotoxic protein–oleic acid complexes, which we have termed liprotides (lipids and partially denatured proteins). Twelve liprotides formed from seven structurally unrelated proteins and prepared by different procedures all displayed core–shell structures, each with a micellar OA core and a shell consisting of flexible, partially unfolded protein, which stabilizes the OA micelle. The common structure explains similar effects exerted on cells by different liprotides and is consistent with a cargo off‐loading of the OA into cell membranes.     

Lipase‐mediated hydrolysis of flax seed oil for selective enrichment of α‐linolenic acid

Polyunsaturated fatty acids (PUFA) are important ingredients of human diet because of their prominent role in the function of human brain, eye and kidney. α‐Linolenic acid (ALA), a C18, n‐3 PUFA is a precursor of long chain PUFA in humans. Commercial lipases of Candida rugosa, Pseudomonas cepacea, Pseudomonas fluorescens, and Rhizomucor miehei were used for hydrolysis of flax seed oil. Reversed phase high performance liquid chromatography followed by gas chromatography showed that the purified oil contained 12 triacylglycerols (TAGs) with differences in fatty acid compositions. Flax seed oil TAGs contained α‐linolenic acid (50%) as a major fatty acid while palmitic, oleic, linoleic made up rest of the portion. Among the four commercial lipases C. rugosa has preference for ALA, and that ALA was enriched in free fatty acids. C. rugosa lipase mediated hydrolysis of the TAGs resulted in a fatty acid mixture that was enriched in α‐linolenic to about 72% yield that could be further enriched to 80% yield by selective removal of saturated fatty acids by urea complexation. Such purified ALA can be used for preparation of ALA‐enriched glycerides. Practical applications : This methodology allows purifying ALA from fatty acid mixture obtained from flax seed oil by urea complexation.     

Dietary trans α‐linolenic acid does not inhibit Δ5‐ and Δ6‐desaturation of linoleic acid in man

Dietary trans monoenes have been associated with an increased risk of heart disease in some studies and this has caused much concern. Trans polyenes are also present in the diet, for example, trans α‐linolenic acid is formed during the deodorisation of α‐linolenic acid‐rich oils such as rapeseed oil. One would expect the intake of trans α‐linolenic acid to be on the increase since the consumption of rapeseed oil in the western diet is increasing. There are no data on trans α‐linolenic acid consumption and its effects. We therefore carried out a comprehensive study to examine whether trans isomers of this polyunsaturated fatty acid increased the risk of coronary heart disease. Since inhibition of Δ6‐desaturase had also been linked to heart disease, the effect of trans α‐linolenic acid on the conversion of [U‐¹³C]‐labelled linoleic acid to dihomo‐γ‐linolenic and arachidonic acid was studied in 7 healthy men recruited from the staff and students of the University of Edinburgh. Thirty percent of the habitual fat was replaced using a trans ‘free’‐ or ‘high’ trans α‐linolenic acid fat. After at least 6 weeks on the experimental diets, the men received 3‐oleyl, 1,2‐[U‐¹³C]‐linoleyl glycerol (15 mg twice daily for ten days). The fatty acid composition of plasma phospholipids and the incorporation of ¹³C‐label into n‐6 fatty acids were determined at day 8, 9 and 10 and after a 6‐week washout period by gas chromatography‐combustion‐isotope ratio mass spectrometry. Trans α‐linolenic acid of plasma phospholipids increased from 0.04 ? 0.01 to 0.17 ? 0.02 and cis ? ‐linolenic acid decreased from 0.42 ? 0.07 to 0.29 ? 0.08 g/100 g of fatty acids on the high trans diet. The composition of the other plasma phospholipid fatty acids did not change. The enrichment of phosphatidyl ¹³C‐linoleic acid reached a plateau at day 10 and the average of the last 3 days did not differ between the low and high trans period. Both dihomo‐γ‐linolenic and arachidonic acid in phospholipids were enriched in ¹³C, both in absolute and relative terms (with respect to ¹³C‐linoleic acid). The enrichment was slightly and significantly higher during the high trans period (P<0.05). Our data suggest that a diet rich in trans α‐linolenic acid (0.6% of energy) does not inhibit the conversion of linoleic acid to dihomo‐γ‐linolenic and arachidonic acid in healthy middle‐aged men consuming a diet rich in linoleic acid.     

Baker's Yeast Deficient in Storage Lipid Synthesis Uses cis‐Vaccenic Acid to Reduce Unsaturated Fatty Acid Toxicity

The role of cis‐vaccenic acid (18:1n‐7) in the reduction of unsaturated fatty acids toxicity was investigated in baker's yeast Saccharomyces cerevisiae. The quadruple mutant (QM, dga1Δ lro1Δ are1Δ are2Δ) deficient in enzymes responsible for triacylglycerol and steryl ester synthesis has been previously shown to be highly sensitive to exogenous unsaturated fatty acids. We have found that cis‐vaccenic acid accumulated during cultivation in the QM cells but not in the corresponding wild type strain. This accumulation was accompanied by a reduction in palmitoleic acid (16:1n‐7) content in the QM cells that is consistent with the proposed formation of cis‐vaccenic acid by elongation of palmitoleic acid. Fatty acid analysis of individual lipid classes from the QM strain revealed that cis‐vaccenic acid was highly enriched in the free fatty acid pool. Furthermore, production of cis‐vaccenic acid was arrested if the mechanism of fatty acids release to the medium was activated. We also showed that exogenous cis‐vaccenic acid did not affect viability of the QM strain at concentrations toxic for palmitoleic or oleic acids. Moreover, addition of cis‐vaccenic acid to the growth medium provided partial protection against the lipotoxic effects of exogenous oleic acid. Transformation of palmitoleic acid to cis‐vaccenic acid is thus a rescue mechanism enabling S. cerevisiae cells to survive in the absence of triacylglycerol synthesis as the major mechanism for unsaturated fatty acid detoxification.     

Anti-mutagenic Properties of Mono- and Dienoic Acid Biohydrogenation Products from Beef Fat

Unsaturated fatty acid biohydrogenation products from beef fat and pure fatty acids were subjected to the Ames Salmonella mutagenicity testing, including monounsaturated fatty acids [MUFA: oleic acid, vaccenic acid, elaidic acid; beef fatty acid fractions rich in trans (t)11/t13‐t14‐18:1 (t11,13,14‐Frac), t10‐18:1 (t10‐Frac)] and dienoic fatty acids [linoleic acid, conjugated linoleic isomers cis (c)9,t11‐18:2 and t10,c12‐18:2, and a mixed beef dienoic fatty acid fraction high in c9,t13‐/t8,c12/t11c15‐18:2 (MD)]. Significantly higher anti‐mutagenic effects of oleic acid, vaccenic acid, t11, 13, 14‐Frac, and t10‐Frac against daunomycin were observed at 2.5 mg. All dienoic acids except MD significantly reduced daunomycin mutagenicity at ≥0.25 mg. Anti‐mutagenicity of oleic and vaccenic acids against 2‐aminoanthracene was found at 2.5 and 0.25 mg, respectively. All dienoic acids significantly reduced 2‐aminoanthracene mutagenicity at ≥0.25 mg. Findings of this study show that unsaturated fatty acids, including trans‐fatty acids commonly found in beef, can act as strong anti‐mutagens.     

Determination of the fatty acid profile by 1H‐NMR spectroscopy

The common unsaturated fatty acids present in many vegetable oils (oleic, linoleic and linolenic acids) can be quantitated by ¹H‐nuclear magnetic resonance spectroscopy (¹H‐NMR). A key feature is that the signals of the terminal methyl group of linolenic acid are shifted downfield from the corresponding signals in the other fatty acids, permitting their separate integration and quantitation of linolenic acid. Then, using the integration values of the signals of the allylic and bis‐allylic protons, oleic and linoleic acids can be quantitated. The procedure was verified for mixtures of triacylglycerols (vegetable oils) and methyl esters of oleic, linoleic and linolenic acids as well as palmitic and stearic acids. Generally, the NMR (400 MHz) results were in good agreement with gas chromatographic (GC) analyses. As the present ¹H‐NMR‐based procedure can be applied to neat vegetable oils, the preparation of derivatives for GC would be unnecessary. The present method is extended to quantitating saturated (palmitic and stearic) acids, although in this case the results deviate more strongly from actual values and GC analyses. Alternatives to the iodine value (allylic position equivalents and bis‐allylic position equivalents) can be derived directly from the integration values of the allylic and bis‐allylic protons.     

Site-specific differences in the fatty acid composition of human adipose tissue

The fatty acid composition of triacylglycerols from fifteen distinct adipose depots taken from each of seven adult male human subjects was compared. Oleic, palmitic, linoleic, stearic, myristic, palmitoleic and vaccenic acids accounted for more than 90% of the triacylglycerol fatty acids in all sites from all subjects; a number of other fatty acids were also identified and quantified. There were large differences in theaverage fatty acid composition between individual subjects. There were no site-specific differences in the proportions of myristic (3.8–4.7% of triacylglycerol fatty acids), palmitic (23–29%), linoleic (6.7–9.8%) or vaccenic (4.1–4.7%) acids or in the proportions of any of the less abundant fatty acids. There were some significant site-specific differences in the proportions of palmitoleic, oleic and stearic acids. The calf depot contained more palmitoleic acid (6.41±1.09%) than the trapezius (3.12±0.55%), perirenal (3.59±0.50%) and mesenteric (3.70±0.43%) depots, more oleic acid (42.13±1.27%) than the trapezius (36.03±2.18%), perirenal (36.50±1.56%) and breast (37.13±1.55%) depots and less stearic acid (5.18±0.89%) than the trapezius (8.57±0.97%), perirenal (8.49±0.75%), mesenteric (7.87±0.42%), breast (8.02±0.75%) and clavicular (8.34±0.78%) depots. The buttock depot contained less stearic acid (6.06±0.65%) than the perirenal, mesenteric and clavicular depots, while the anterior thigh depot contained less stearic acid (6.07±0.70%) than the perirenal depot. These findings indicate that, while most human adipose depots differ little in fatty acid composition, some sites, in particular the calf, perirenal, trapezius and mesenteric depots, have site-specific properties.     

The fatty acid composition of lipids from muscle and adipose tissues of pigs fed various oil mixtures differing in their ratio between oleic acid and linoleic acid

High concentrations of polyunsaturated fatty acids (PUFA) in meat have detrimental effects on its technical properties. The present study was carried out to investigate whether PUFA levels in pork can be reduced by increasing the concentrations of oleic acid in pig diets. To this end a bifactorial experiment was carried out with 48 female growing finishing pigs. Six different diets were used with two different concentrations of linoleic acid (12 vs. 24 g/kg) and three different concentrations of oleic acid (12 vs. 18 vs. 24 g/kg). The experiment started at a body weight (BW) of 58 kg and continued until 115 kg BW. The fatty acid composition of total lipids of backfat, perirenal fat and musculus (m.) longissimus dorsi was analysed. Concentrations of linoleic acid and total PUFA in backfat and perirenal fat were affected only by the dietary linoleic acid content but not at all by the dietary oleic acid content. Increasing the dietary concentration of oleic acid raised the level of oleic acid in those tissues at the expense of saturated fatty acids, suggesting competition between monounsaturated fatty acids and saturated fatty acids for incorporation into triglycerides. At the low dietary linoleic acid concentration, the percentages of linoleic acid and total PUFA in total lipids of m. longissimus dorsi were also unaffected by the dietary oleic acid content. In contrast, at the high dietary linoleic acid concentration, percentages of linoleic acid and total PUFA of the m. longissimus dorsi were reduced by increasing the dietary concentration of oleic acid, suggesting that oleic acid and linoleic acid compete for incorporation into muscle lipids. Thus, at high dietary linoleic acid levels the fatty acid composition of the m. longissimus dorsi was favourably affected by high dietary oleic acid concentrations; in backfat and perirenal fat, however, no beneficial effect of high dietary oleic acid levels was seen.     

The hydrolysis of fatty acid chlorides

Summary Fatty acid chlorides of octanoic, decanoic, lauric, myristic, palmitic, stearic, oleic, elaidic, and linoleic acids were hydrolyzed at 25° C, in water and the amounts of unchanged acid chlorides determined after different periods of reaction. Contrary to expectations, the chlorides of the longer chain fatty acids, palmitic and stearic, reacted at a more rapid rate than the chlorides of the shorter chain fatty acids. Lauryl chloride appears to be more resist-ant to hydrolysis than either the chlorides of the lower molecular weight octanoic and decanoic acids or the chlorides of the higher molecular weight myristic to stearic acids. The chlorides of the unsaturated acids, oleic, elaidic, and linoleic, are hydrolyzed less rapidly than stearyl chloride. However, elaidyl and myristyl chlorides exhibit the same relative rates of hydrolysis during the first two hours of reaction. Myristyl chloride hydrolyzes more rapidly than elaidyl chloride after the first two hours. The addition of either hydrochloric acid or free fatty acids to the reaction mixture was found to have no pronounced effect on the hydrolysis of the acid chlorides. One of the laboratories of the Bureau of Agricultural and Industrial Chemistry, Agricultural Research Administration, U. S. Department of Agriculture.     

Circadian rhythm of fatty acid desaturation in mouse liver

A study was made of the diurnal changes in liver microsomal desaturation of labeled stearic, linoleic and α-linolenic acids to oleic, γ-linolenic and octadeca-6,9,12,15-tetraenoic acids, respectively. C3H-S mice were used and were exposed to light-dark cycles. A circadian rhythm was observed for stearic acid desaturation, and a different one for linoleic acid. Linoleic and α-linolenic desaturation had similar responses in the day cycle. This would indicate that different mechanisms control the oxidative desaturations of the fatty acids in the 9 and 6 carbons. The fatty acid composition of the whole liver and liver microsomes also showed variations. Remarkable oscillations were observed for stearic and oleic acids. Neither the total protein synthesis nor the free fatty acid concentration in the microsomes followed a rhythm parallel to the desaturation of the studied fatty acids. The injection of cycloheximide 4 hr before measuring the desaturation modified the circadian variation of both the 9 and 6 desaturations. The modification induced by cycloheximide was considered to indicate that both variations are related to the synthesis of specific proteins but not to that of a degradative or inhibitory protein.     

Definite influence of location and climatic conditions on the fatty acid composition of sunflower seed oil

Percentages of linoleic, oleic and stearic acids present significant differences between growing areas, whereas palmitic acid content remains practically constant, or at least presents no significant relation to the growing area. Nevertheless, palmitic acid appears to follow a pattern that relates its content to the total content of the other three major fatty acids. Seeds grown in the northern part of Spain presented a higher linoleic content than seeds grown in the South, which is in agreement with the general theory found in prior studies. Although there is an inverse correlation between oleic and linoleic content, we have found that the total content of both is neither constant nor independent of temperature, and increases when temperature and oleic acid increase. However, stearic content increases when the combination of linoleic and oleic acid decreases, suggesting a total constant value for the combination of these three acids. The average temperature of the are during development of the seed and the local climatic conditions have the greatest influence over fatty acid composition, while the seed variety presents limited influence.     

Lipids of cultured hepatoma cells: VI. Glycerolipid and monoenoic fatty acid biosynthesis in minimal deviation hepatoma 7288C

1-14C-Acetic, 1-14C-palmitic, or 1-14C-stearic acid was incubated with minimal deviation hepatoma 7288C cells grown in culture to assess: de novo fatty acid synthesis, oxidation, desaturation, and elongation of saturated fatty acids, as well as the ability of media fatty acids to serve as precursors of cellular glycerolipids. Distribution of radioactivity in the individual lipid classes and the various fatty acids of triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was determined. The radioactivity among the monoenoic acid isomers derived from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was analyzed by reductive ozonolysis. Only small amounts of the labeled substrates were oxidized to carbon dioxide. Except for labeled stearic acid, which also was incorporated heavily into phosphatidyl inositol and phosphatidyl serine, most radioactivity was recovered in triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine. Synthesis of cholesterol and long chain fatty acids from labeled acetic acid demonstrated that these cells can perform de novo synthesis of fatty acids and cholesterol. Both labeled palmitic and stearic acids were desaturated to the corresponding delta9 monoenes, and palmitic and palmitoleic acids were elongated. The nexadecenoic acid fraction isolated from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine, when acetic or palmitic acid was the labeled substrate, showed that greater than 70 percent of the labeled acids were the delta9 isomer. Radioactivity of the octadecenoic acid fraction derived from labeled acetic or palmitic acids was nearly equally divided between the delta9 isomer, oleic acid, and the delta11 isomer, vaccenic acid. Desaturation of labeled stearic acid produced only oleic acid. These data demonstrate that the biosynthesis of vaccenic acid in these cultured neoplastic cells proceeds via the elongation of palmitoleic acid. The relatively high level of vaccenic acid synthesis in these cells suggests that the reported elevation of "oleic acid" in many neoplasms may result from increased concentration of vaccenic acid.     

Surface-active properties of sodium salts of sulfated fatty acid monoglycerides

Summary Sodium salts of fatty acid monoglyceride sulfates have been prepared by sulfating purified monoglycerides with chlorosulfonic acid or a pyridine-sulfur trioxide complex and subsequent neutralizing. Surface tension, interfacial tension, wetting, suspending and foaming characteristics, calcium stability, and emulsifying property (including stability of the emulsion obtained) of the aqueous solution of these surfactants from C₁₂, C₁₄, C₁₆, and C₁₈ saturated fatty acids and from oleic acid and linoleic acids have been determined and evaluated. With the exception of the wetting characteristic which was found to be optimum in the case of the more hydrophilic products (like those from lauric and linoleic acids) the remaining properties were found to reach a maximum value when the hydrophilic-hydrophobic balance in the surfactant molecule was seemingly optimum, as attained by myristic and oleic acid products.     

Commercial Runner peanut cultivars in the USA: Fatty acid composition

Though peanuts are classified as a high‐fat food, they possess good proportions of fatty acids deemed as heart healthy. The fatty acid compositions of Runner peanuts were determined for commercially grown cultivars over two recent crop years. GC‐FID analyses revealed that the fatty acid levels for Runner peanuts were significantly (p <0.05) different among the normal, mid‐, and high‐oleic peanuts investigated. Oleic acid‐to‐linoleic acid (O/L) ratios were found to be 1.93 ± 0.30, 5.25 ± 1.12, and 16.9 ± 5.20 for normal, mid‐, and high‐oleic peanut lipids, respectively. Tamrun OL01 possessed a fatty acid profile characteristic of a mid‐oleic cultivar. From the sample set (n = 151), mean % weights for oleic acid and linoleic acid were 52.09 ± 2.84 and 27.38 ± 2.60 in normal, 69.33 ± 3.18 and 13.66 ± 2.35 in mid‐oleic, and 78.45 ± 2.05 and 5.11 ± 1.67 in high‐oleic peanuts, respectively. Cluster analysis segregated cultivars based on fatty acids into normal, mid‐, and high‐oleic groups. Factorial analysis revealed that cultivar effects were significant (p <0.01) for all fatty acids, except for lignoceric acid. Cultivar effects were also highly significant (p <0.001) for O/L, IV, unsaturated/saturated fatty acid (U/S) ratio, and % saturation. Significant crop year effects were shown for palmitic, oleic, arachidic, gondoic, and lignoceric acids, as well as U/S ratio and % saturation. Healthy unsaturated fats accounted for ?80% in all crop years and cultivars.     

Comparison of fatty acid content of imported peanuts

Variability in fatty acid compositions of peanuts imported from six different countries into the United States were studied to determine their effect on processing and storage conditions. The oil content ranged from 44.1 to 50.4%. Major fatty acids, palmitic acid (C16:0), oleic acid (C18:l), and linoleic acid (C18:2) ranged from 8.6 to 12.7, 35.9 to 61.1 and 21.7 to 44.2%, respectively. Oleic and lino-leic acids together comprised ca. 78.0–83.0% of the total fatty acids. Highly significant differences (P<.01) in fatty acid compositions were obtained between samples and between locations (countries of origin). Indicators of stability of the peanut samples as measured by the oleic/linoleic acid ratio (O/L) and iodine value (IV) of the extracted peanut oils showed variable but significant differences (P <.05) between locations. Generally, higher O/L ratios corresponding to lower IV indicate better stability and longer shelf-life of the samples.     

Oxidized fatty acid-protein complexes

Summary Complexes have been formed between egg albumin and oxidized linoleic acid. Little or no complex formation could be obtained with unoxidized linoleic acid, oleic acid, or lauric acid. The amount of complexed linoleic acid could not be increased to more than 8.0% in spite of a long reaction time. The number of reactive groups (amino, sulfhydryl, and hydroxyl) in the protein of the complexes and in the original protein were found to be the same. The data seemed to indicate that a covalent linkage did not exist between the reactive groups of the protein and the lipide in complexes of this type. Strongly bound adsorption complexes were formed between alumina and oxidized lipides by a simple mixing technique. A possible structure on the basis of a large number of hydrogen bonds has been proposed for the lipide-protein and the lipide-alumina complexes and has been discussed in detail. Portion of a thesis presented by K. A. Narayan as partial fulfillment of the requirements for the degree of Doctor of Philosophy in Food Technology. Supported by a grant-in-aid from Swift and Company and by research grant No. C-1932 from the National Institute of Health. U. S. Public Health Service, Department of Health, Education and Welfare.     

Determination of fatty acids and some undesirable fatty acid isomers in selected Turkish margarines

The fatty acid composition and total trans fatty acid content in 10 margarines produced in Turkey were determined by capillary gas chromatography and Fourier transform‐infrared spectroscopy (FT‐IR) spectroscopy. The fatty acid composition ranged as follows: saturated fatty acids, C16:0 (palmitic) 11.3 to 31.8% and C18:0 (stearic) 5.7 to 8.7%, monounsaturated fatty acids, C18:1 (oleic) 21.8 to 35.7% and C18:1 trans isomers 0.4 to 27.4%, polyunsaturated fatty acid, C18:2 linoleic acid 5.2 to 40.2%. Some positional isomers of C18:1 as cis‐11‐octadecenoic acid varied from 0.7 to 4.6% and cis‐13 trace to 2.4%. The total trans fatty acid contents were between 0.9 and 32.0% when measured with capillary gas chromatography and between 0 and 30.2% with FT‐IR spectroscopy. Some of the margarines analyzed contained trace amount of trans fatty acids which could not be detected by FT‐IR spectroscopy.     

Die Bestimmung einiger Kennzahlen von freien Fettsäuren natürlicher Fette nach γ-Bestrahlung

Some Characteristic Values of Free Acids of Natural Fats after Irradiation with γ-Rays The alteration of some characteristic values of palmitic, stearic, linoleic and oleic acids after irradiation with γ-rays at 25, 40, 60 and 90 Mrad was investigated. With increasing dose of irradiation the acid value indicated a falling tendency in all cases, whereas the iodine value after γ-irradiation showed varying values. Benzidine value which could be measured at 25 Mrad only, showed a slight increase. At the highest dose of irradiation, peroxide value of saturated and unsaturated fatty acids behaved in different manner; compared to the value obtained at 40 Mrad, a relatively strong increase was observed with saturated fatty acids and a rather considerable decrease was found with unsaturated fatty acids. The refractive index of oleic and linoleic acids increased steadily, corresponding to the dose of irradiation on individual fatty acids.     

The effect of fatty acid composition of rapeseed oil on plasma lipids and oxidative stability of low‐density lipoproteins in cholesterol‐fed hamsters

We studied the effect of four rapeseed oils with different fatty acid profiles on parameters implicated in the pathogenesis of atherosclerosis in humans in a model experiment with hamsters. The hamsters were divided into seven groups and fed a semi‐synthetic, cholesterol‐enriched diet (5 g/kg diet) containing 15% of the fat in question for a period of six weeks. The following rapeseed oils were used: (1) conventional rapeseed oil (6% saturated fatty acids [SFA], 64% monounsaturated fatty acids [MUFA], 18% linoleic acid [LA], 9% α‐linolenic acid [ALA]), (2) linoleic acid‐rich rapeseed oil (6% SFA, 61% MUFA, 28% LA, 2% ALA), (3) oleic acid‐rich rapeseed oil (6% SFA, 74% MUFA, 11% LA, 5% ALA), (4) myristic acid‐rich rapeseed oil (11% myristic acid, 35% SFA, 44% MUFA, 14% LA, 5% ALA). Sunflower oil, olive oil and lard were used as control fats. The concentrations of the lipids in the plasma, in the lipoprotein fractions and in the liver, the fatty acid composition of various tissues, the tocopherol status and the susceptibility of low‐density lipoproteins (LDL) to in vitro‐oxidation were determined. The concentrations of total cholesterol found in the plasma and in the LDL fraction and the ratios of LDL to HDL were similar after feeding the four different types of rapeseed oil, sunflower oil and olive oil. Lard produced the highest concentrations of cholesterol in plasma and the LDL fraction and the highest ratio of LDL to HDL. Feeding conventional, oleic acid‐ and myristic acid‐rich rapeseed oils resulted in markedly lower ratios of arachidonic to eicosapentaenoic acid in the lipids of the liver and the erythrocytes. This is considered beneficial for the formation of eicosanoids. The lag‐time before the onset of peroxidation of the LDL lipids, induced by copper ions, was not statistically significant between the seven hamster groups suggesting that the susceptibility of LDL to lipid peroxidation was similar after feeding all types of fat. Considering all parameters obtained in the used hamster model it is obvious that all four rapeseed oils are at least as favourable as olive oil or sunflower oil.     

Stability of pumpkin seed oil

In Austria pumpkins are grown primarily for the production of pumpkin seeds that can be used for eating or the production of salad oil. Pumpkin seed oil is dark green and its fatty acid composition consists typically of linoleic acid and oleic acid as the dominant fatty acids. The saturated fatty acids palmitic and stearic acid occur at lower levels. The samples for this study were taken from a breeding program that intends to increase the seed and oil productivity. 15 samples with different contents of linoleic acid (40—57%) and vitamin E (100—600 μg/g) were selected. The stability of the oil was measured in a Rancimat that oxidizes the oil at 120 �C and measures the induction time that is needed for the oxidation. The correlation analysis showed that only the ratio of linoleic acid to oleic acid had a significant influence on the oxidative stability of the oil. Vitamin E did not show any correlation. When α‐tocopherol was added to the oil a strong pro‐oxidative effect was observed.